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Effects Of Heat-Conduction Dry Needling Therapy On TRPV1 Channel In Rats

PURPOSE: This study was aimed to investigate the effects of heat-conduction dry needling therapy on chronic myofascial pain syndrome (CMPS) in rats and explore the analgesic mechanisms by measuring the mRNA expression of transient receptor potential cation channel subfamily V member 1 (TRPV1) in mus...

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Autores principales: Wang, Gang, Wang, Xinglin, Gao, Qian, Wang, Ning, Zhou, Ming
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800561/
https://www.ncbi.nlm.nih.gov/pubmed/31686903
http://dx.doi.org/10.2147/JPR.S225900
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author Wang, Gang
Wang, Xinglin
Gao, Qian
Wang, Ning
Zhou, Ming
author_facet Wang, Gang
Wang, Xinglin
Gao, Qian
Wang, Ning
Zhou, Ming
author_sort Wang, Gang
collection PubMed
description PURPOSE: This study was aimed to investigate the effects of heat-conduction dry needling therapy on chronic myofascial pain syndrome (CMPS) in rats and explore the analgesic mechanisms by measuring the mRNA expression of transient receptor potential cation channel subfamily V member 1 (TRPV1) in musculus gastrocnemius. METHODS: Seventy-two rats were randomly divided into five groups. Group A was the control group containing eight normal rats. Group B was the model group where 16 rats developed CMPS in musculus gastrocnemius but received no treatments. Groups C, D, and E containing 16 CMPS rats in each group were the trial groups receiving heat-conduction dry needling therapy. In detail, rats in Group C received dry needling treatment at the heating temperature of 44°C. Rats in Group D received intramuscular injection of capsazepine before receiving dry needling treatment with the heating temperature at 44°C. Rats in Group E received dry needling treatment with the heating temperature at 40°C. The mRNA expression of TRPV1, protein kinase C (PKC), and interleukin (IL)-6 in the needle insertion points of musculus gastrocnemius was measured at 24 hrs and 7 days after dry needling therapy. RESULTS: Compared with untreated CMPS rats, the mRNA expression of TRPV1, PKC, and interleukin-6 (IL-6) was increased in rats receiving dry needling therapy with the heating temperature at 44°C for 24 hrs. However, the mRNA expression of TRPV1, PKC, and IL-6 in CMPS rats receiving injection of TRPV1 antagonist capsazepine into musculus gastrocnemius followed by temperature-needling at 44°C was analogous to that in untreated CMPS rats. CONCLUSION: Dry needling therapy with needles heated to 44°C could impact the activity of TRPV1/PKC/IL-6 pathway.
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spelling pubmed-68005612019-11-04 Effects Of Heat-Conduction Dry Needling Therapy On TRPV1 Channel In Rats Wang, Gang Wang, Xinglin Gao, Qian Wang, Ning Zhou, Ming J Pain Res Original Research PURPOSE: This study was aimed to investigate the effects of heat-conduction dry needling therapy on chronic myofascial pain syndrome (CMPS) in rats and explore the analgesic mechanisms by measuring the mRNA expression of transient receptor potential cation channel subfamily V member 1 (TRPV1) in musculus gastrocnemius. METHODS: Seventy-two rats were randomly divided into five groups. Group A was the control group containing eight normal rats. Group B was the model group where 16 rats developed CMPS in musculus gastrocnemius but received no treatments. Groups C, D, and E containing 16 CMPS rats in each group were the trial groups receiving heat-conduction dry needling therapy. In detail, rats in Group C received dry needling treatment at the heating temperature of 44°C. Rats in Group D received intramuscular injection of capsazepine before receiving dry needling treatment with the heating temperature at 44°C. Rats in Group E received dry needling treatment with the heating temperature at 40°C. The mRNA expression of TRPV1, protein kinase C (PKC), and interleukin (IL)-6 in the needle insertion points of musculus gastrocnemius was measured at 24 hrs and 7 days after dry needling therapy. RESULTS: Compared with untreated CMPS rats, the mRNA expression of TRPV1, PKC, and interleukin-6 (IL-6) was increased in rats receiving dry needling therapy with the heating temperature at 44°C for 24 hrs. However, the mRNA expression of TRPV1, PKC, and IL-6 in CMPS rats receiving injection of TRPV1 antagonist capsazepine into musculus gastrocnemius followed by temperature-needling at 44°C was analogous to that in untreated CMPS rats. CONCLUSION: Dry needling therapy with needles heated to 44°C could impact the activity of TRPV1/PKC/IL-6 pathway. Dove 2019-10-15 /pmc/articles/PMC6800561/ /pubmed/31686903 http://dx.doi.org/10.2147/JPR.S225900 Text en © 2019 Wang et al. http://creativecommons.org/licenses/by-nc/3.0/ This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Wang, Gang
Wang, Xinglin
Gao, Qian
Wang, Ning
Zhou, Ming
Effects Of Heat-Conduction Dry Needling Therapy On TRPV1 Channel In Rats
title Effects Of Heat-Conduction Dry Needling Therapy On TRPV1 Channel In Rats
title_full Effects Of Heat-Conduction Dry Needling Therapy On TRPV1 Channel In Rats
title_fullStr Effects Of Heat-Conduction Dry Needling Therapy On TRPV1 Channel In Rats
title_full_unstemmed Effects Of Heat-Conduction Dry Needling Therapy On TRPV1 Channel In Rats
title_short Effects Of Heat-Conduction Dry Needling Therapy On TRPV1 Channel In Rats
title_sort effects of heat-conduction dry needling therapy on trpv1 channel in rats
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6800561/
https://www.ncbi.nlm.nih.gov/pubmed/31686903
http://dx.doi.org/10.2147/JPR.S225900
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